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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 16, 2007
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autismChrista Lese Martin, Jacqueline A Duvall, Yesim Ilkin, et al.
JAMA Neurology|August 19, 2014
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxiaBrent L Fogel, Hane Lee, Joshua L Deignan, et al.
Iscience|February 22, 2021
Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factorsTimothy S Chang, Yi Ding, Malika K Freund, et al.
Science Translational Medicine|January 23, 2015
Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autismOlga Peñagarikano, María T Lázaro, Xiao-Hong Lu, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2023
The contributions of rare inherited and polygenic risk to ASD in multiplex familiesMatilde Cirnigliaro, Timothy S Chang, Stephanie A Arteaga, et al.
Science (New York, N.Y.)|August 18, 2022
Functional regulatory variants implicate distinct transcriptional networks in dementiaYonatan A Cooper, Noam Teyssier, Nina M Dräger, et al.
Nucleic Acids Research|March 14, 2015
Genome engineering of isogenic human ES cells to model autism disordersRefugio A Martinez, Jason L Stein, Anne-Rachel F Krostag, et al.
Annals of Neurology|December 14, 2011
A gene expression phenotype in lymphocytes from Friedreich ataxia patientsGiovanni Coppola, Ryan Burnett, Susan Perlman, et al.
Cardiovascular and Interventional Radiology|October 20, 2011
Transcatheter treatment of hepatocellular carcinoma with Doxorubicin-loaded DC Bead (DEBDOX): technical recommendationsRiccardo Lencioni, Thierry de Baere, Marta Burrel, et al.
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